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以RNA为中心的方法来描绘选定RNA上的RNA-蛋白质相互作用图谱。

RNA-Centric Approaches to Profile the RNA-Protein Interaction Landscape on Selected RNAs.

作者信息

Gerber André P

机构信息

Department of Microbial Sciences, School of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford GU2 7XH, UK.

出版信息

Noncoding RNA. 2021 Feb 15;7(1):11. doi: 10.3390/ncrna7010011.

Abstract

RNA-protein interactions frame post-transcriptional regulatory networks and modulate transcription and epigenetics. While the technological advances in RNA sequencing have significantly expanded the repertoire of RNAs, recently developed biochemical approaches combined with sensitive mass-spectrometry have revealed hundreds of previously unrecognized and potentially novel RNA-binding proteins. Nevertheless, a major challenge remains to understand how the thousands of RNA molecules and their interacting proteins assemble and control the fate of each individual RNA in a cell. Here, I review recent methodological advances to approach this problem through systematic identification of proteins that interact with particular RNAs in living cells. Thereby, a specific focus is given to in vivo approaches that involve crosslinking of RNA-protein interactions through ultraviolet irradiation or treatment of cells with chemicals, followed by capture of the RNA under study with antisense-oligonucleotides and identification of bound proteins with mass-spectrometry. Several recent studies defining interactomes of long non-coding RNAs, viral RNAs, as well as mRNAs are highlighted, and short reference is given to recent in-cell protein labeling techniques. These recent experimental improvements could open the door for broader applications and to study the remodeling of RNA-protein complexes upon different environmental cues and in disease.

摘要

RNA-蛋白质相互作用构成了转录后调控网络,并调节转录和表观遗传学。虽然RNA测序技术的进步显著扩展了RNA的种类,但最近开发的生化方法与灵敏的质谱技术相结合,揭示了数百种以前未被识别且可能是新的RNA结合蛋白。然而,一个主要挑战仍然是要了解数千种RNA分子及其相互作用的蛋白质如何在细胞中组装并控制每个RNA分子的命运。在此,我回顾了最近通过系统鉴定活细胞中与特定RNA相互作用的蛋白质来解决这一问题的方法学进展。因此,特别关注了体内方法,这些方法包括通过紫外线照射或用化学物质处理细胞使RNA-蛋白质相互作用交联,然后用反义寡核苷酸捕获所研究的RNA,并用质谱法鉴定结合的蛋白质。重点介绍了最近几项定义长链非编码RNA、病毒RNA以及mRNA相互作用组的研究,并简要提及了最近的细胞内蛋白质标记技术。这些最近的实验改进可能为更广泛的应用打开大门,并有助于研究在不同环境线索和疾病中RNA-蛋白质复合物的重塑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b034/7930960/d7b095edbb3e/ncrna-07-00011-g001.jpg

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